Simioni P - Search Results

1

Residual platelet factor V ensures thrombin generation in patients with severe congenital factor V deficiency and mild bleeding symptoms.

Duckers C, Simioni P, Spiezia L, Radu C, Dabrilli P, Gavasso S, Rosing J, Castoldi E. Duckers C, et al. Among authors: simioni p. Blood. 2010 Jan 28;115(4):879-86. doi: 10.1182/blood-2009-08-237719. Epub 2009 Oct 27. Blood. 2010. PMID: 19861681 Free article.

2

A protein S functional assay yields unsatisfactory results in patients with activated protein C resistance.

Simioni P, Gavasso S, Luni S, Invidiato S, Girolami A. Simioni P, et al. Blood Coagul Fibrinolysis. 1995 May;6(3):286-7. doi: 10.1097/00001721-199505000-00014. Blood Coagul Fibrinolysis. 1995. PMID: 7654942 No abstract available.

3

Prothrombin fragment 1+2 and thrombin-antithrombin complex levels in patients with inherited APC resistance due to factor V Leiden mutation.

Simioni P, Scarano L, Gavasso S, Sardella C, Girolami B, Scudeller A, Girolami A. Simioni P, et al. Br J Haematol. 1996 Feb;92(2):435-41. doi: 10.1046/j.1365-2141.1996.d01-1500.x. Br J Haematol. 1996. PMID: 8603014

4

An in vitro analysis of the combination of hemophilia A and factor V(LEIDEN).

van 't Veer C, Golden NJ, Kalafatis M, Simioni P, Bertina RM, Mann KG. van 't Veer C, et al. Among authors: simioni p. Blood. 1997 Oct 15;90(8):3067-72. Blood. 1997. PMID: 9376587 Free article.

5

Platelet-derived factor Va/Va Leiden cofactor activities are sustained on the surface of activated platelets despite the presence of activated protein C.

Camire RM, Kalafatis M, Simioni P, Girolami A, Tracy PB. Camire RM, et al. Among authors: simioni p. Blood. 1998 Apr 15;91(8):2818-29. Blood. 1998. PMID: 9531592 Free article.

6

Molecular bases of pseudo-homozygous APC resistance: the compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasma.

Castoldi E, Kalafatis M, Lunghi B, Simioni P, Ioannou PA, Petio M, Girolami A, Mann KG, Bernardi F. Castoldi E, et al. Among authors: simioni p. Thromb Haemost. 1998 Sep;80(3):403-6. Thromb Haemost. 1998. PMID: 9759618

7

Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family.

Castoldi E, Simioni P, Kalafatis M, Lunghi B, Tormene D, Girelli D, Girolami A, Bernardi F. Castoldi E, et al. Among authors: simioni p. Blood. 2000 Aug 15;96(4):1443-8. Blood. 2000. PMID: 10942390 Free article.

8

Risk for subsequent venous thromboembolic complications in carriers of the prothrombin or the factor V gene mutation with a first episode of deep-vein thrombosis.

Simioni P, Prandoni P, Lensing AW, Manfrin D, Tormene D, Gavasso S, Girolami B, Sardella C, Prins M, Girolami A. Simioni P, et al. Blood. 2000 Nov 15;96(10):3329-33. Blood. 2000. PMID: 11071624 Free article.

9

A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders.

Castoldi E, Lunghi B, Mingozzi F, Simioni P, Girolami A, Bernardi F. Castoldi E, et al. Among authors: simioni p. Br J Haematol. 2001 Sep;114(4):868-70. doi: 10.1046/j.1365-2141.2001.03052.x. Br J Haematol. 2001. PMID: 11564076 Free article.

10

Incidence of venous thromboembolism in asymptomatic family members who are carriers of factor V Leiden: a prospective cohort study.

Simioni P, Tormene D, Prandoni P, Zerbinati P, Gavasso S, Cefalo P, Girolami A. Simioni P, et al. Blood. 2002 Mar 15;99(6):1938-42. doi: 10.1182/blood.v99.6.1938. Blood. 2002. PMID: 11877263 Free article.

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